BEUDAMED
    12 results · 50ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    SONESTA

    FDA Adverse Event
    Injury ·SONESTA MEDICAL AB·Product code IXR·January 9, 2026

    SOLESTA

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LNM·July 9, 2014

    SOLESTA

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LNM·April 7, 2014

    SOLESTA

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LNM·May 29, 2014

    SOLESTA

    FDA Adverse Event
    Injury ·A-MED AB·Product code LNM·February 4, 2013

    SOLESTA

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LNM·January 15, 2014

    SOLESTA

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LNM·November 28, 2012

    SOLESTA

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LNM·February 25, 2015

    SOLESTA

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LNM·December 18, 2012

    SOLESTA

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LNM·April 10, 2013

    SOLESTRA

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LNM·April 7, 2014

    SOLESTA

    FDA Adverse Event
    Injury ·Q-MED AB·Product code LNM·April 15, 2013